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WO2003035627A1 - Derives de piperazine a activite antagoniste du recepteur ccr1 - Google Patents

Derives de piperazine a activite antagoniste du recepteur ccr1 Download PDF

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Publication number
WO2003035627A1
WO2003035627A1 PCT/IB2002/003989 IB0203989W WO03035627A1 WO 2003035627 A1 WO2003035627 A1 WO 2003035627A1 IB 0203989 W IB0203989 W IB 0203989W WO 03035627 A1 WO03035627 A1 WO 03035627A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
oxo
piperazin
benzyl
fluoro
Prior art date
Application number
PCT/IB2002/003989
Other languages
English (en)
Inventor
Laura Cook Blumberg
Matthew Frank Brown
Matthew Merrill Hayward
Christopher Stanley Poss
Gregory Dean Lundquist, Jr.
Andre Shavnya
Original Assignee
Pfizer Products Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to CA002463272A priority Critical patent/CA2463272C/fr
Priority to JP2003538143A priority patent/JP2005507923A/ja
Priority to KR10-2004-7005885A priority patent/KR20040047941A/ko
Priority to APAP/P/2004/003008A priority patent/AP2004003008A0/en
Priority to EEP200400088A priority patent/EE200400088A/xx
Priority to SK185-2004A priority patent/SK1852004A3/sk
Priority to DK02772651.2T priority patent/DK1438298T3/da
Priority to EA200400466A priority patent/EA006243B1/ru
Priority to HU0401735A priority patent/HUP0401735A3/hu
Priority to BR0213452-7A priority patent/BR0213452A/pt
Priority to EP02772651A priority patent/EP1438298B1/fr
Priority to MXPA04002423A priority patent/MXPA04002423A/es
Application filed by Pfizer Products Inc. filed Critical Pfizer Products Inc.
Priority to AT02772651T priority patent/ATE456559T1/de
Priority to DE60235249T priority patent/DE60235249D1/de
Publication of WO2003035627A1 publication Critical patent/WO2003035627A1/fr
Priority to IS7180A priority patent/IS7180A/is
Priority to HR20040289A priority patent/HRP20040289A2/hr
Priority to TNP2004000072A priority patent/TNSN04072A1/fr
Priority to NO20041631A priority patent/NO20041631L/no

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
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    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/76—Nitrogen atoms to which a second hetero atom is attached
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79—Acids; Esters
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79—Acids; Esters
    • C07D213/80—Acids; Esters in position 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C07D213/82—Amides; Imides in position 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/34—One oxygen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/60—Three or more oxygen or sulfur atoms
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    • C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182—Radicals derived from carboxylic acids
    • C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/32—Oxygen atoms
    • C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
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    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Definitions

  • the present invention relates to novel piperazine derivatives, methods of use and pharmaceutical compositions containing them.
  • the compounds of the invention are potent and selective inhibitors of MIP-1 ⁇ (CCL3) binding to its receptor CCR1 found on inflammatory and immunomodulatory cells (preferably leukocytes and lymphocytes).
  • CCR1 found on inflammatory and immunomodulatory cells (preferably leukocytes and lymphocytes).
  • the CCR1 receptor is also sometimes referred to as the CC-CKR1 receptor.
  • MIP-1 ⁇ and the related chemokines shown to interact with CCR1 (e.g., RANTES (CCL5), MCP-2 (CCL8), MCP-3 (CCL7), HCC-1 (CCL14) and HCC-2 (CCL15))) induced chemotaxis of THP-1 cells and human leukocytes and are potentially useful for the treatment or prevention of autoimmune diseases (such as rheumatoid arthritis, type I diabetes (recent onset), lupus, inflammatory bowel disease, optic neuritis, psoriasis, multiple sclerosis, polymyalgia rheumatica, uveitis, and vasculitis), acute and chronic inflammatory conditions (such as osteoarthritis, adult Respiratory Distress Syndrome, Respiratory Distress Syndrome of infancy, ischemia reperfusion injury, and glomerulonephritis), allergic conditions (such as asthma and atopic dermatitis), inflammation associated with infection (such as viral inflammation
  • CCR1
  • Compounds in this series may also limit the production of cytokines at inflammatory sites, including but not limited to TNF and IL-1 , as a consequence of decreasing cell infiltration, providing benefit for diseases linked to TNF and IL-1 , including congestive heart failure, pulmonary emphysema or dyspnea associated therewith, emphysema; HIV-1 , HIV-2, HIV-3; cytomegalovirus (CMV), adenoviruses, Herpes viruses (Herpes zoster and Herpes simplex).
  • CMV cytomegalovirus
  • Herpes viruses Herpes zoster and Herpes simplex
  • TNF inflammatory cytokines
  • TNF e.g, fungal meningitis, joint tissue damage, hyperplasia, pannus formation and bone resorption, psoriatic arthritis, hepatic failure, bacterial meningitis, Kawasaki syndrome, myocardial infarction, acute liver failure, lyme disease, septic shock, cancer, trauma, and malaria, etc.
  • MIP-1 ⁇ and RANTES are soluble chemotactic peptides (chemokines) which are produced by a variety of cell types, including inflammatory cells, such as CD8+ lymphocytes, polymorphonuclear leukocytes (PMNs) and macrophages, J.Biol. Chem.. 270 (30) 29671-29675 (1995). These chemokines act by inducing the migration and activation of key inflammatory and immunomodulatory cells. Elevated levels of chemokines have been found in the synovial fluid of rheumatoid arthritis patients, chronic and rejecting tissue from transplant patients and in the nasal secretions of allergic rhinitis patients following allergen exposure (Teran , et al., J. Immunol..).
  • Preferred compounds of formula I include those wherein each R 1 is independently H-, HO-, halo, NC-, (d-C 8 )alkyl-, or (d-C 8 )alkyl-O-.
  • Other preferred compounds of formula I include those wherein each R 2 and
  • Y is a pyridyl ring.
  • Propane-2-sulfonic acid [(5-chloro-2- ⁇ 2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5- dimethyl-piperazin-1-yl]-2-oxo-ethoxy ⁇ -phenyl)-acetyl]-amide.
  • the compound of formula I is: (2- ⁇ 2-[4-(4-Fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-2-oxo-ethoxy ⁇ -5- trifluoromethyl-phenyl)-methanesulfonamide;
  • the compound of formula I is: (2S)-2-Amino-4-(5-chloro-2- ⁇ 2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl- piperazin-1 -yl]-2-oxo-ethoxy ⁇ -phenoxy)-butyric acid;
  • the compound of formula I is: (2R)-2-(5-Chloro-2- ⁇ 2-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-2-oxo- ethoxy ⁇ -phenoxy)-propionic acid;
  • the present invention also relates to pharmaceutical compositions comprising an amount of a compound of the formula I or a pharmaceutically acceptable form thereof and a pharmaceutically acceptable carrier.
  • another aspect of the present invention relates to using the aforementioned compounds of formula I wherein the use comprises administering a pharmaceutically effective amount of a compound of formula I, or a pharmaceutically acceptable form thereof, to a mammal to treat or prevent a disorder or condition selected from autoimmune diseases, lupus, acute and chronic inflammatory conditions, allergic conditions, inflammation associated with infection, viral, chronic bronchitis, xeno-transplantation, transplantation tissue rejection, atherosclerosis, restenosis, HIV infectivity, and granulomatous diseases.
  • autoimmune diseases lupus, acute and chronic inflammatory conditions, allergic conditions, inflammation associated with infection, viral, chronic bronchitis, xeno-transplantation, transplantation tissue rejection, atherosclerosis, restenosis, HIV infectivity, and granulomatous diseases.
  • the present invention relates to the use of compounds according to formula I, wherein the use comprises administering a pharmaceutically effective amount of a compound of formula I, or a pharmaceutically acceptable form thereof, to a mammal to treat or prevent a disorder or condition that can be treated or prevented by antagonizing the CCR1 receptor in a mammal.
  • another aspect of the present invention relates to the use of compositions comprising compounds of formula I or pharmaceutically acceptable forms thereof, wherein the use comprises administering a pharmaceutically effective amount of the composition a mammal to treat or prevent a disorder or condition that can be treated or prevented by antagonizing the CCR1 receptor in a mammal.
  • the acids which are used to prepare the pharmaceutically acceptable acid addition salts of the aforementioned base compounds of this invention are those which form non-toxic acid addition salts, Le., salts containing pharmacologically acceptable anions, such as the hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, acetate, lactate, citrate, acid citrate, tartrate, bitartrate, succinate, maleate, fumarate, gluconate, saccharate, benzoate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate and pamoate (i.e., 1 ,1'-methylene-bis-(2-hydroxy-3- naphthoate)) salts.
  • pharmacologically acceptable anions such as the hydrochloride, hydrobromide, hydroiodide, nitrate,
  • the invention also relates to base addition salts of formula I.
  • the chemical bases that may be used as reagents to prepare pharmaceutically acceptable base salts of those compounds of formula I that are acidic in nature are those that form nontoxic base salts with such compounds.
  • Such non-toxic base salts include, but are not limited to those derived from such pharmacologically acceptable cations such as alkali metal cations (e.g., potassium and sodium) and alkaline earth metal cations (e.g.. calcium and magnesium), ammonium or water-soluble amine addition salts such as N- methylglucamine-(meglumine), and the lower alkanolammonium and other base salts of pharmaceutically acceptable organic amines.
  • the compounds of this invention may contain olefin-like double bonds. When such bonds are present, the compounds of the invention exist as cis and trans configurations and as mixtures thereof.
  • This invention also includes isotopically-labeled compounds, which are identical to those described by Formula I, except for the fact that one or more atoms are replaced by one or more atoms having specific atomic mass or mass numbers.
  • isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, sulfur, and fluorine, such as 2 H, 3 H, 13 C, 14 C, 15 N, 18 0, 17 O, and 18 F, respectively.
  • Compounds of the present invention, prodrugs thereof, and pharmaceutically acceptable salts of the compounds or of the prodrugs which contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of this invention.
  • isotopically-labeled compounds of the present invention for example those into which radioactive isotopes such as 3 H and 14 C are incorporated, are useful in drug and/or substrate tissue distribution assays. Tritiated (i.e., 3 H), and carbon-14 (i.e., 14 C), isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with heavier isotopes such as deuterium (i.e., 2 H), can afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements and, hence, may be preferred in some circumstances.
  • Isotopically labeled compounds of Formula I of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes and/or in the Examples below, by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.
  • alkyl referred to herein may be linear or branched, a and they may also be cyclic (e.g.. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl) or bicyclic (e.g., norbornanyl, bicyclo [3.2.1]octane) or contain cyclic groups.
  • alkyl includes alkyl radicals, generally known as alkylenes, including, but not limited to, methylene, ethylene, propylene, and the like.
  • alkenyl referred to herein may be linear or branched, and they may also be cyclic (e.g. cyclobutenyl, cyclopentenyl, cyclohexenyl) or bicyclic or contain cyclic groups.
  • Aryl refers to phenyl or naphthyl which may be optionally substituted with 1 , 2 or 3 substituents independently selected from the group consisting of but not limited to: H-, HO-, halo-, (d-C ⁇ )alkyh (d-C ⁇ )alkyl-O-, HO-(d-C 8 )alkyl-, NC-, H 2 N-, (C
  • halo or halogen includes fluorine, chlorine, bromine, and iodine.
  • Heterocyclyl refers to but is not limited to lactone, lactam, diazepanyl, pyrrolidinyl, tetrahydrofuranyl, dihydrofuranyl, tetrahydropyranyl, pyranyl, thiopyranyl, aziridinyl, oxiranyl, methylenedioxyl, chromenyl, barbituryl, isoxazolidinyl, 1 ,3- oxazolidin-3-yl, isothiazolidinyl, 1 ,3-thiazolidin-3-yl, 1 ,2-pyrazolidin-2-yl, 1 ,3-pyrazolidin- 1-yl, piperidinyl, thiomorpholinyl, 1 ,2-tetrahydrothiazin-2-yl, 1 ,3-tetrahydrothiazin-3-yl, tetrahydrothiadiazinyl, morpholinyl, 1 ,2-tetrahydr
  • Said heterocyclyl group at least one carbon atom, wherein the heteroatoms may be any combination of N, O, or S.
  • Heteroaryl refers but is not limited to furyl, thienyl, thiazolyl, pyrazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, triazolyl, tetrazolyl, imidazolyl, 1 ,3,5- oxadiazolyl, 1 ,2,4-oxadiazolyl, 1 ,2,3-oxadiazolyl, 1 ,3,5-thiadiazolyl, 1 ,2,3-thiadiazolyl, 1 ,2,4-thiadiazolyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, 1 ,2,4-triazinyl, 1 ,2,3-triazinyl, 1 ,3,5-triazinyl, pyrazolo[3,4-b]pyridinyl, cinnolinyl, pteridinyl,
  • Said heteroaryl group contains at least one carbon atom, wherein the heteroatoms may be any combination of N, O, or S.
  • pharmaceutically acceptable is meant a material that is not biologically or otherwise undesirable, i.e., the material may be administered to an individual without causing any substantially undesirable biological effects or interacting in a deleterious manner with any of the other components of a pharmaceutical composition in which it may be contained.
  • “Pharmaceutically acceptable forms” when used herein refers to any pharmaceutically acceptable derivative or variation, including conformational isomers (e.g., cis and trans isomers) and all optical isomers (e.g.. enantiomers and diastereomers), racemic, diastereomeric and other mixtures of such isomers, as well as solvates, hydrates, isomorphs, polymorphs, tautomers, esters, salt forms, and prodrugs.
  • tautomers is meant chemical compounds that may exist in two or more forms of different structure (isomers) in equilibrium, the forms differing, usually, in the position of a hydrogen atom.
  • Various types of tautomerism can occur, including keto-enol, ring-chain and ring-ring tautomerism.
  • reaction Schemes illustrate the preparation of the compounds of the present invention. Unless otherwise indicated a, b, c, d, and R 1 through R 6 and structural formula I in the reaction Schemes and the discussion that follow are defined as above.
  • R 7 refers to an amino radical that can be unsubstituted, monosubstituted, disubstituted, cyclic or acyclic.
  • the reactions in the Preparations and Schemes are described in commonly assigned co-pending application serial no. USSN: 09/821322, filed March 29, 2001 , and provisional copending application serial no. 60/241804 filed October 19, 2000, the disclosures of which are incorporated herein by reference in their entirties for all purposes.
  • reaction mixture is stirred at room temperature for a time period between about 1 hour to about 4 hours, preferably about 2 hours.
  • reaction 2 of Preparation A the compound of formula III is converted to the corresponding compound of formula IV by first reacting a compound of the formula
  • reaction 3 of Preparation A the compound of formula IV is converted to the corresponding piperizine-2,5-dione compound of formula V by treating IV with trifluoroacetic acid in the presence of a polar aprotic solvent, such as methylene chloride.
  • a polar aprotic solvent such as methylene chloride.
  • reaction 4 of Preparation A the compound of formula V is converted to the corresponding compound of formula VI by reducing V with a reducing agent, such as lithium aluminum hydride.
  • a reducing agent such as lithium aluminum hydride.
  • the reaction is conducted at a temperature between about -10°C to about 10°C, preferably about 0°C, for a time period between about 10 minutes to about 90 minutes, preferably about 40 minutes.
  • reaction 5 of Preparation A the compound of formula VI is converted to the corresponding compound of formula VII by reacting VI with chloroacetyl chloride in the presence of a base, such as triethylamine, in a polar aprotic solvent, such as methylene chloride, at ambient temperature for a time period between 15 minutes and 3 hours, preferably about 30 minutes.
  • a base such as triethylamine
  • a polar aprotic solvent such as methylene chloride
  • the compound of formula VI is converted to the corresponding compound of formula VIII by reacting VI with acetoxy acetylchloride in the presence of a base, such as triethylamine, in a polar aprotic solvent, such as methylene chloride, at ambient temperature for a time period between 15 minutes and 4 hours, preferably about 1 hour.
  • a base such as triethylamine
  • a polar aprotic solvent such as methylene chloride
  • the resulting acetyl-protected alcohol is reacted with lithium hydroxide hydrate in a solvent mixture including water, tetrahydrofuran and methanol, at ambient temperature for a time period between 1 hour and 8 hours, preferably about 2 hours.
  • the compound of formula VI is converted to the corresponding compound of formula IX by reacting VI with N-(t- butoxycarbonyl)glycine in the presence of a base, such as dimethylamino pyridine and a coupling reagent, such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimine, in a polar aprotic solvent, such as methylene chloride, at ambient temperature for a time period between 4 hours and 18 hours, preferably about 12 hours.
  • a base such as dimethylamino pyridine
  • a coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimine
  • the resulting compound containing an N-(t-butoxycarbonyl) protecting group is reacted with trifluoroacetic acid in a polar aprotic solvent, such as methylene chloride, at ambient temperature for a time period between 30 minutes and 6 hours, preferably about 2 hours.
  • a polar aprotic solvent such as methylene chloride
  • Preparation A allows access to all the various isomers, diastereomers and enantiomers of formula VI.
  • Preparation A can be utilized to prepare compounds with the preferred stereochemistry as depicted in the formula:
  • reaction 1 of Preparation B the compound of formula X is converted to the corresponding compound of formula XI by reacting X with an appropriate amine in the presence of a polar aprotic solvent, such as tetrahydrofuran.
  • a polar aprotic solvent such as tetrahydrofuran.
  • the reaction mixture is stirred at ambient temperature for a time period between about 1 hour to about 24 hours, preferably about 12 hours.
  • reaction 2 of Preparation B the compound of formula XI is converted to the corresponding compound of formula XII by reacting XI with thiophenol in the presence of a base, such as sodium hydride, and a polar aprotic solvent, such as dimethylformamide.
  • a base such as sodium hydride
  • a polar aprotic solvent such as dimethylformamide
  • reaction 1 of Preparation C the compound of formula XIII, where e is 1-4, is converted to the corresponding compound of formula XIV by first converting the hydroxyl group to a chloro group by reacting XIII with thionyl chloride, in the presence of an aprotic solvent, such as methylene chloride.
  • an aprotic solvent such as methylene chloride.
  • the reaction is heated to reflux, for a time period between about 1 hour to about 10 hours, preferably about 3 hours.
  • the resulting alkyl chloride is then treated with thioacetic acid in the presence of a base, such as cesium carbonate, in a polar aprotic solvent, such as dimethylformamide at ambient temperature for a time period between 6 hours and 24 hours, preferably about 12 hours.
  • reaction 2 of Preparation C the compound of formula XIV is converted to the corresponding compound of formula XV by reacting XIV with hydrogen peroxide (aqueous solution) in acetic acid at ambient temperature for a time period between 6 hours and 24 hours, preferably about 12 hours.
  • reaction 3 of Preparation C the compound of formula XV is converted to the corresponding compound of formula XVI by first reacting XV with phosphorous pentachloride in an aprotic solvent, such as toluene, at a temperature between ambient and reflux, preferably at reflux for a time period between 1 hour and 8 hours, preferably 3 hours to give the corresponding sulfonyl chloride. The sulfonyl chloride is then reacted with an appropriate amine in a polar aprotic solvent, such as tetra hydrofu ran, at ambient temperature for a time period between 3 hours and 24 hours, preferably 12 hours.
  • aprotic solvent such as toluene
  • reaction 4 of Preparation C the compound of formula XVI is converted to the corresponding compound of formula XVII according to the procedure described in reaction 2 of Preparation B.
  • reaction 1 of Preparation D the compound of formula XVIII is converted to the corresponding compound of the formula XIX by treating XVIII with a reducing agent, such as lithium aluminum hydride, in an aprotic solvent, such as tetrahydrofuran.
  • a reducing agent such as lithium aluminum hydride
  • an aprotic solvent such as tetrahydrofuran.
  • the reaction mixture is heated to reflux for a time period between 1 hour and 6 hours, preferably about 2 hours.
  • reaction 2 of Preparation D the compound of formula XIX is converted to the corresponding compound of the formula XX by first converting the hydroxyl group to a chloro group by reacting XIX with thionyl chloride, in the presence of an aprotic solvent, such as methylene chloride.
  • an aprotic solvent such as methylene chloride.
  • the reaction is heated to reflux, for a time period between about 1 hour to about 10 hours, preferably about 3 hours.
  • the resulting alkyl chloride is then treated with a cyanide source, such as potassium cyanide, in the presence of an aprotic solvent, such as acetonitrile and a crown ether, such as 18-crown-6.
  • a cyanide source such as potassium cyanide
  • reaction 3 of Preparation D the compound of formula XX is converted to the compound of formula XXI by treating XX with a hydroxide source, such as potassium hydroxide in a mixture of ethanol and water.
  • a hydroxide source such as potassium hydroxide in a mixture of ethanol and water.
  • the reaction mixture is heated to reflux for a time period between about 1 hour to about 10 hours, preferably about 8 hours.
  • reaction 4 of Preparation D the compound of formula XXI is converted to the compound of formula XXII, wherein f is 1 , by first demethylating the methyl ether by treatment with acid, such as 47% aqueous hydrogen bromide.
  • the reaction mixture is heated to reflux for a time period between about 10 hours to about 30 hours, preferably about 24 hours.
  • the phenolic acid is finally converted to the corresponding compound of formula XXII, wherein f is 1 , by treating with ethanol in the presence of an acid, such as hydrochloric acid, at ambient temperature for a time period between about 8 hours to about 16 hours, preferably about 12 hours.
  • reaction 5 of Preparation D the compound of formula XIX is converted to the corresponding compound of formula XXIII, by treating XIX with an oxidizing agent, such as Dess-Martin periodinane, in the presence of an aprotic solvent, such as tetrahydrofuran at ambient temperature for a time period between about 1 hour to about 16 hours, preferably about 4 hours.
  • an oxidizing agent such as Dess-Martin periodinane
  • an aprotic solvent such as tetrahydrofuran
  • g is 1 - 7, in the presence of an aprotic solvent, such as tetrahydrofuran.
  • an aprotic solvent such as tetrahydrofuran.
  • the reaction is conducted at a temperature between -78 °C and reflux, the preferred temperature is dependent on which phosphonium ylide is utilized, for a time period between about 4 hours to about 16 hours, preferably about 10 hours (for similar transformations, see: J. Am. Chem. Soc. 1985, 107, 217).
  • the resulting olefinic ester is then hydrogenated by shaking under a positive pressure of hydrogen in the presence of a catalyst, such as platinum dioxide, in the presence of an aprotic solvent such as ethyl acetate.
  • the methyl ether is then deprotected according to the procedure described in reaction 2 of Preparation B.
  • a base such as 4- dimethylaminopyridine
  • a coupling reagent such as 1-(3-dimethylaminopropyl)- 3-ethylcarbodiimine
  • the compound of formula VI is converted to the corresponding compound of formula I by first reacting VI with a compound of the formula: in the presence of an aprotic solvent, such as toluene, at a temperature between ambient and reflux, preferably reflux, for a time period between about 4 hours to 18 hours, preferably about 12 hours.
  • an aprotic solvent such as toluene
  • reaction 1 of Scheme 2 the compound of formula VII is converted to the corresponding compound of formula XXIV by reacting VII with a compound of the formula, H-X-Y[(R 5 ) d ](NO 2 ) wherein X is -O-, -S-, or -NH- in the presence of potassium carbonate, potassium iodide and an aprotic solvent, such as butanone.
  • the reaction is heated to reflux for a time period between about 4 hours to about 8 hours, preferably about 6 hours.
  • reaction 2 of Scheme 2 the compound of formula XXIV is converted to the corresponding compound of formula XXV by hydrogenating XXIV in the presence of a catalyst, such as platinum on carbon, and a polar protic solvent, such as ethanol.
  • a catalyst such as platinum on carbon
  • a polar protic solvent such as ethanol.
  • the reaction is carried out under a pressure between about 30 psi to about 40 psi, preferably about 35 psi, for a time period between about 5 minutes to about 1 hour, preferably 30 minutes.
  • reaction 3 of Scheme 2 the compound of formula XXV is converted to the corresponding urea of formula I, by first reacting XXV with 4-nitrophenyl chloroformate in the presence of a base, such as pyridine, and a polar aprotic solvent, such as methlyene chloride, followed by reacting the intermediate so formed with an appropriate amine or sulfonamide.
  • a base such as pyridine
  • a polar aprotic solvent such as methlyene chloride
  • the compound of formula XXV is reacted with an appropriate sulfonyl chloride to form the corresponding sulfonamides of formula I, in the presence of a base, such as triethylamine, and a polar aprotic solvent, such as methylene chloride. The reaction is stirred overnight at ambient temperature.
  • a base such as triethylamine
  • a polar aprotic solvent such as methylene chloride.
  • the compound of formula XXV is reacted with an appropriate aldehyde in the presence of a base, such as triethylamine, and a reducing agent, such as sodium triacetoxyborohydride, in an aprotic solvent, such as 1 ,2-dichloroethane.
  • reaction 1 of Scheme 3 the compound of formula VII is converted to the corresponding compound of formula XXVI where h is 0 - 3 according to the procedure described above in reaction 1 of Scheme 2.
  • reaction 2 of Scheme 3 the compound of formula XXVI is converted to the corresponding amine of formula I by reacting XXVI with an appropriate amine in the presence of a 10:1 ratio solution of dichloroethane/acetic acid.
  • the reaction mixture is stirred, at ambient temperature, for a time period between about 30 minutes to about 2 hours, preferably about 1 hour.
  • a reducing agent such as sodium cyanoborohydride is than added to the mixture and the reaction is allowed to stir overnight at ambient temperature. If the amine thus formed is primary or secondary, the compound of formula I may further be reacted according to the procedure described above in reaction 3 of Scheme 2, to provide ureas or sulfonamides.
  • the compound of formula XXVI is converted to the corresponding oxime of formula I by reacting XXVI with an appropriate alkoxyamine in the presence of a base, such as triethylamine and a polar protic solvent, such as methanol, at a temperature between 0° C and reflux, preferably at ambient temperature, for a time period between 1 hour and 8 hours, preferably about 3 hours.
  • a base such as triethylamine
  • a polar protic solvent such as methanol
  • reaction 1 of Scheme 4 the compound of formula VII is converted to the corresponding compound of formula XXVII by reacting VII with a compound of the formula, H-X-Y[(R 5 ) d ](CH 2 )iCO 2 Et, wherein X is -O-, -S-, or -NH- and i is 0 - 3, according to the procedure described in reaction 1 of Scheme 2.
  • reaction 2 of Scheme 4 the compound of formula XXVII is converted to the corresponding compound of formula XXVIII by reacting XXVII with a reducing agent, such as sodium borohydride, in a polar protic solvent, such as methanol, at ambient temperature for a time period between about 1 hour to about 10 hours, preferably about 3 hours.
  • a reducing agent such as sodium borohydride
  • a polar protic solvent such as methanol
  • reaction 3 of Scheme 4 the compound of formula XXVIII is converted to the corresponding ether of formula I by first converting XXVIII to the corresponding alkyl chloride as described in reaction 2 of Preparation D.
  • the alkyl chloride is then reacted with an appropriate alcohol which has previously been reacted with a strong base, such as NaH, in a polar aprotic solvent, such as dimethylformamide at a temperature between about -10 °C to about 10 °C, preferably about 0 °C, for a time period between about 10 minutes to about 90 minutes, preferably about 40 minutes.
  • the alkyl chloride is stirred with the resulting alkoxide at ambient temperature for a period of about 3 hours to about 24 hours, preferably about 12 hours.
  • the compound of formula XXVIII is converted to the corresponding carbamate of formula I by reacting XXVIII with an appropriate isocyanate in the presence of a base, such as triethylamine, in an aprotic solvent, such as toluene, at ambient temperature for a time period between 4 hours and 24 hours, preferably about 12 hours.
  • a base such as triethylamine
  • aprotic solvent such as toluene
  • the compound of formula XXVIII is converted to the corresponding acylsulfamide of formula I by first reacting XXVIII with a BOC-protected sulfamide, such as tert- butoxycarbonylsulfamide in the presence of triphenylphosphine and diethylazodicarboxylate in a polar aprotic solvent, such as tetrahydrofuran.
  • a BOC-protected sulfamide such as tert- butoxycarbonylsulfamide
  • triphenylphosphine and diethylazodicarboxylate such as tetrahydrofuran.
  • the reaction is initially conducted at a temperature between - 100 °C and 0 °C, preferably about -60 °C for a time period of about 15 minutes, then slowly warmed to a temperature between 10 °C and ambient temperature for a time period between 1 hour and 8 hours, preferably about 2 hours.
  • the resulting BOC-protected sulfamide is reacted with an acyl chloride in the presence of a base, such as triethyl amine and/or dimethylpyridine in a polar aprotic solvent, such as dichloromethane.
  • a base such as triethyl amine and/or dimethylpyridine
  • a polar aprotic solvent such as dichloromethane.
  • the reaction is stirred at a temperature between 0 °C and 40 °C, preferably at ambient temperature for a time period of 8 hours to 24 hours, preferably about 18 hours.
  • the BOC-protected acylsulfamide thus formed is treated with a strong acid, such as trifluoracetic acid, in a polar aprotic solvent, such as dichloromethane, at ambient temperature for a time period between 1 hour and 6 hours, preferably about 3 hours, thus giving compounds of formula I.
  • reaction 4 of Scheme 4 the compound of formula XXVII is converted to the corresponding compound of formula I by reacting XXVII with lithium hydroxide monohydrate in the presence of methanol, tetrahydrofuran and water to give the corresponding carboxylic acid.
  • the reaction mixture is stirred at ambient temperature for a time period between 8 and 24 hours, preferably 12 hours.
  • the carboxylic acid is converted to the corresponding acylsulfonamide of formula I by reacting the carboxylic acid with an appropriate sulfonamide in the presence of a base, such as 4-dimethylaminopyridine and coupling reagent, such as 1-(3- dimethylaminopropyl)-3-ethylcarbodiimine, in a polar aprotic solvent, such as methylene chloride.
  • a base such as 4-dimethylaminopyridine
  • coupling reagent such as 1-(3- dimethylaminopropyl)-3-ethylcarbodiimine
  • the carboxylic acid is converted to the corresponding acylsulfamide of formula I by reacting the carboxylic acid with chlorosulfonylisocyanate in a polar aprotic solvent, such as 1 ,2- dichloroethane, at a temperature between ambient and reflux, preferably ambient, for a time period between 8 and 24 hours, preferably about 12 hours, to give a compound of formula:
  • a polar aprotic solvent such as 1 ,2- dichloroethane
  • a polar aprotic solvent such as tetrahydrofuran
  • reaction 1 of Scheme 5 the compound of formula VII is converted to the corresponding compound of formula XXIX by reacting VII with a compound of the formula, H-X-Y[(R 5 ) d ](CH 2 ) j SO 2 NH 2 , wherein X is -O-, -S-, or -NR 6 - and j is 0 - 4, according to the procedure described in reaction 1 of Scheme 2.
  • reaction 2 of Scheme 5 the compound of formula XXIX is converted to the corresponding acylsulfonamide of formula I by reacting XXIX with an appropriate carboxylic acid in the presence of a base, such as 4-dimethylaminopyridine, and a coupling reagent, such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimine, in a polar aprotic solvent, such as methylene chloride.
  • a base such as 4-dimethylaminopyridine
  • a coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimine
  • the compound of formula XXIX is converted to the corresponding sulfonylurea of formula I by reacting XXIX with an appropriate isocyanate in the presence of a base, such as 1 ,8-diazobicyclo[5.4.0]undec-7-ene and a polar aprotic solvent, such as tetrahydrofuran.
  • a base such as 1 ,8-diazobicyclo[5.4.0]undec-7-ene
  • a polar aprotic solvent such as tetrahydrofuran.
  • the compound of formula XXIX is converted to the corresponding sulfonylcarbamate of formula I by reacting XXIX with an appropriate chloroformate in the presence of a base, such as 1 ,8-diazobicyclo[5.4.0]undec-7-ene and a polar aprotic solvent, such as tetrahydrofuran.
  • a base such as 1 ,8-diazobicyclo[5.4.0]undec-7-ene
  • a polar aprotic solvent such as tetrahydrofuran.
  • the compound of formula XXIX is converted to the corresponding alkylated sulfonamide of formula I by first treating compound XXIX with di-t-butyl-dicarbonate in the presence of base such as triethylamine and 4-dimethylaminopyridine in a polar aprotic solvent such as dichloromethane.
  • base such as triethylamine and 4-dimethylaminopyridine
  • a polar aprotic solvent such as dichloromethane.
  • the resulting N-t-butyloxycarbonyl protected sulfonamide is then treated with an alkyl halide in the presence of a polar, aprotic solvent such as dimethylformamide.
  • N-t-butyloxycarbonyl protected secondary sulfonamide is then deprotected by treating with acid, such as trifluoroacetic acid in the presence of a polar solvent such as dichloromethane.
  • acid such as trifluoroacetic acid
  • a polar solvent such as dichloromethane.
  • reaction 1 of Scheme 6 the compound of formula VIII is converted to the corresponding compound of formula I by reacting VIII with a strong base, such as sodium hydride, in an aprotic solvent, such as toluene, at a temperature between about -10 °C and ambient temperature, preferably about 0 °C for a time period between 15 minutes and 90 minutes, preferably about 30 minutes.
  • the reactants are stirred at a temperature between ambient and reflux, preferably ambient temperature for a time period between 8 hours and 24 hours, preferably 12 hours.
  • the compound of formula IX is converted to the corresponding compound of formula I where R 6 is H-, by reacting IX with a compound of formula CI-Y[(R 5 ) d ](R 4 ) where Y is a (C C 9 ) heteroaryl wherein the chlorine is attached to a carbon atom that is adjacent to a heteroatom (for example, 2-pyridyl).
  • the reactants are stirred in a polar aprotic solvent, such as acetonitrile, in the presence of a base, such as triethylamine, at reflux temperature for a time period between about 4 hours and 24 hours, preferably about 12 hours.
  • the compound of formula I where R 6 is H- is converted to the compound of formula I where R 6 is an alkyl group by reacting the compound of formula I where R 6 is H- with an appropriate alkyl halide in the presence of a base, such as triethylamine, and a polar aprotic solvent, such as tetrahydrofuran at a temperature between ambient and reflux, preferably at ambient temperature for a time period of 8 hours to 24 hours, preferably about 18 hours.
  • a base such as triethylamine
  • a polar aprotic solvent such as tetrahydrofuran
  • the compound of formula I where R 6 is H- is converted to the compound of formula I where R 6 taken together with the nitrogen to which it is attached forms an amide, by reacting the compound of formula I where R 6 is H- with an appropriate carboxylic acid in the presence of a base, such as 4- dimethylaminopyridine, and a coupling reagent, such as 1-(3-dimethylaminopropyl)- 3-ethylcarbodiimine, in a polar aprotic solvent, such as methylene chloride.
  • a base such as 4- dimethylaminopyridine
  • a coupling reagent such as 1-(3-dimethylaminopropyl)- 3-ethylcarbodiimine
  • the compound of formula I where R 6 is H- is converted to the compound of formula I where R 6 taken together with the nitrogen to which it is attached forms a urea, by reacting the compound of formula I where R 6 is H- with an appropriate isocyanate in the presence of a base, such as triethyamine, and a polar aprotic solvent, such as tetrahydrofuran.
  • a base such as triethyamine
  • a polar aprotic solvent such as tetrahydrofuran
  • the compound of formula I where R 6 is H- is converted to the compound of formula I where R 6 taken together with the nitrogen to which it is attached forms a carbamate, by reacting the compound of formula I where R 6 is H- with an appropriate chloroformate in the presence of a base, such as triethyamine, and a polar aprotic solvent, such as tetrahydrofuran.
  • a base such as triethyamine
  • a polar aprotic solvent such as tetrahydrofuran
  • the compound of formula I where R 6 is H- is converted to the compound of formula I where R 6 taken together with the nitrogen to which it is attached forms a sulfonamide, by reacting the compound of formula I where R 6 is H- with an appropriate sulfonylchloride in the presence of a base, such as triethyamine, and a polar aprotic solvent, such as tetrahydrofuran.
  • a base such as triethyamine
  • a polar aprotic solvent such as tetrahydrofuran.
  • the reaction is stirred at a temperature between ambient and reflux, preferably reflux, for a time period of 4 hours to 18 hours, preferably about 12 hours.
  • the pressure of each of the above reactions is not critical. Generally, the reactions will be conducted at a pressure of about one to about three atmospheres, preferably at ambient pressure (about one atmosphere).
  • the compounds of the formula I which are basic in nature are capable of forming a wide variety of different salts with various inorganic and organic acids. Although such salts must be pharmaceutically acceptable for administration to animals, it is often desirable in practice to initially isolate a compound of the formula I from the reaction mixture as a pharmaceutically unacceptable salt and then simply convert the latter back to the free base compound by treatment with an alkaline reagent, and subsequently convert the free base to a pharmaceutically acceptable acid addition salt.
  • the acid addition salts of the base compounds of this invention are readily prepared by treating the base compound with a substantially equivalent amount of the chosen mineral or organic acid in an aqueous solvent medium or in a suitable organic solvent such as methanol or ethanol. Upon careful evaporation of the solvent, a solid salt is obtained.
  • the acids which are used to prepare the pharmaceutically acceptable acid addition salts of the base compounds of this invention are those which form non-toxic acid addition salts, Le., salts containing pharmacologically acceptable anions, such as hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate or bisulfate, phosphate or acid phosphate, acetate, lactate, citrate or acid citrate, tartrate or bitartrate, succinate, maleate, fumarate, gluconate, saccharate, benzoate, methanesulfonate and pamoate (i.e., 1 ,1 '-methylene-bis-(2-hydroxy-3-naphthoate)) salts.
  • pharmacologically acceptable anions such as hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate or bisulfate, phosphate or acid phosphate, acetate, lactate, citrate or acid citrate, tartrate
  • Those compounds of the formula I which are also acidic in nature, are capable of forming base salts with various pharmacologically acceptable cations.
  • such salts include the alkali metal or alkaline-earth metal salts and particularly, the sodium and potassium salts. These salts are all prepared by conventional techniques.
  • the chemical bases which are used as reagents to prepare the pharmaceutically acceptable base salts of this invention are those which form non-toxic base salts with the herein described acidic compounds of formula I. These non-toxic base salts include those derived from such pharmacologically acceptable cations as sodium, potassium, calcium and magnesium, etc.
  • salts can easily be prepared by treating the corresponding acidic compounds with an aqueous solution containing the desired pharmacologically acceptable cations, and then evaporating the resulting solution to dryness, preferably under reduced pressure.
  • they may also be prepared by mixing lower alkanolic solutions of the acidic compounds and the desired alkali metal alkoxide together, and then evaporating the resulting solution to dryness in the same manner as before.
  • stoichiometric quantities of reagents are preferably employed in order to ensure completeness of reaction and maximum product yields.
  • the active compounds are potent antagonists of the CCR1 receptor.
  • the active compounds are useful in the treatment or prevention of autoimmune diseases (such as rheumatoid arthritis, type I diabetes (recent onset), lupus, inflammatory bowel disease, optic neuritis, psoriasis, multiple sclerosis, polymyalgia rheumatica, uveitis, and vasculitis), acute and chronic inflammatory conditions (such as osteoarthritis, adult Respiratory Distress Syndrome, Respiratory Distress Syndrome of infancy, ischemia reperfusion injury, and glomerulonephritis), allergic conditions (such as asthma and atopic dermatitis), infection associated with inflammation (such as viral inflammation (including influenza and hepatitis) and Guillian-Barre syndrome syndrome), chronic bronchitis, xeno- transplantation, transplantation tissue rejection (chronic and acute), organ rejection
  • autoimmune diseases such as rheumatoid arthritis, type I diabetes (recent onset),
  • Compounds in this series may also have utility for the prevention of cancer metastasis.
  • Compounds in this series may also limit the production of cytokines at inflammatory sites, including but not limited to TNF and IL-1 , as a consequence of decreasing cell infiltration, providing benefit for diseases linked to TNF and IL-1 , including congestive heart failure, pulmonary emphysema or dyspnea associated therewith, emphysema; HIV-1 , HIV-2, HIV-3; cytomegalovirus (CMV), adenoviruses, Herpes viruses (Herpes zoster and Herpes simplex).
  • CMV cytomegalovirus
  • Herpes viruses Herpes zoster and Herpes simplex
  • TNF inflammatory cytokines
  • TNF e.g, fungal meningitis, joint tissue damage, hyperplasia, pannus formation and bone resorption, psoriatic arthritis, hepatic failure, bacterial meningitis, Kawasaki syndrome, myocardial infarction, acute liver failure, lyme disease, septic shock, cancer, trauma, and malaria, etc.
  • the activity of the compounds of the invention can be assessed according to procedures know to those of ordinary skill in the art. Examples of recognized methods for determining CCR1 induced migration can be found in Coligan, J. E., Kruisbeek, A.M., Margulies, D.H., Shevach, E.M., Strober, W. editors: Current Protocols In Immunology. 6.12.1- 6.12.3. (John Wiley and Sons, NY, 1991). One specific example of how to determine the activity of a compound for inhibiting migration is described in detail below.
  • the ability of compounds to inhibit the chemotaxis to various chemokines can be evaluated using standard 48 or 96 well Boyden Chambers with a 5 micron polycarbonate filter. All reagents and cells can be prepared in standard RPMI (BioWhitikker Inc.) tissue culture medium supplemented with 1 mg/mL of bovine serum albumin. Briefly, MIP-1 ⁇ (Peprotech, Inc., P.O. Box 275, Rocky Hill NJ) or other test agonists, are placed into the lower chambers of the Boyden chamber. A polycarbonate filter is then applied and the upper chamber fastened. The amount of agonist chosen is that determined to give the maximal amount of chemotaxis in this system (e.g., 1 nM for MIP-1 ⁇ should be adequate).
  • THP-1 cells ATCC TIB-202
  • primary human monocytes or primary lymphocytes
  • Compound dilutions can be prepared using standard serological techniques and are mixed with cells prior to adding to the chamber.
  • the chamber is removed, the cells in the upper chamber aspirated, the upper part of the filter wiped and the number of cells migrating can be determined according to the following method.
  • the chamber (a 96 well variety manufactured by Neuroprobe) can be centrifuged to push cells off the lower chamber and the number of cells can be quantitated against a standard curve by a color change of the dye fluorocein diacetate.
  • the filter For primary human monocytes, or lymphocytes, the filter can be stained with Dif Quik® dye (American Scientific Products) and the number of cells migrating can be determined microscopically.
  • Dif Quik® dye American Scientific Products
  • the number of cells migrating in the presence of the compound are divided by the number of cells migrating in control wells (without the compound).
  • the quotant is the % inhibition for the compound which can then be plotted using standard graphics techniques against the concentration of compound used.
  • the 50% inhibition point is then determined using a line fit analysis for all concentrations tested.
  • the line fit for all data points must have an coefficient of correlation (R squared) of > 90% to be considered a valid assay.
  • compositions of the present invention may be formulated in a conventional manner using one or more pharmaceutically acceptable carriers.
  • the active compounds of the invention may be formulated for oral, buccal, intranasal, parenteral (e.g., intravenous, intramuscular or subcutaneous) or rectal administration or in a form suitable for administration by inhalation or insufflation.
  • the active compounds of the invention may also be formulated for sustained delivery.
  • the pharmaceutical compositions may take the form of, for example, tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g., lactose, microcrystalline cellulose or calcium phosphate); lubricants (e.g., magnesium stearate, talc or silica); disintegrants (e.g., potato starch or sodium starch glycolate); or wetting agents (e.g., sodium lauryl sulphate).
  • binding agents e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose
  • fillers e.g., lactose, microcrystalline cellulose or calcium phosphate
  • lubricants e.g., magnesium stearate, talc or silica
  • disintegrants e.g., potato starch or sodium
  • Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use.
  • Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g., sorbitol syrup, methyl cellulose or hydrogenated edible fats); emulsifying agents (e.g., lecithin or acacia); non-aqueous vehicles (e.g., almond oil, oily esters or ethyl alcohol); and preservatives (e.g., methyl or propyl p-hydroxybenzoates or sorbic acid).
  • the composition may take the form of tablets or lozenges formulated in conventional manner.
  • the active compounds of the invention may be formulated for parenteral administration by injection, including using conventional catheterization techniques or infusion.
  • Formulations for injection may be presented in unit dosage form, e.g.. in ampules or in multi-dose containers, with an added preservative.
  • the compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulating agents such as suspending, stabilizing and/or dispersing agents.
  • the active ingredient may be in powder form for reconstitution with a suitable vehicle, e.g., sterile pyrogen-free water, before use.
  • the active compounds of the invention may also be formulated in rectal compositions such as suppositories or retention enemas, e ⁇ , containing conventional suppository bases such as cocoa butter or other glycerides.
  • the active compounds of the invention are conveniently delivered in the form of a solution or suspension from a pump spray container that is squeezed or pumped by the patient or as an aerosol spray presentation from a pressurized container or a nebulizer, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • the dosage unit may be determined by providing a valve to deliver a metered amount.
  • the pressurized container or nebulizer may contain a solution or suspension of the active compound.
  • Capsules and cartridges for use in an inhaler or insufflator may be formulated containing a powder mix of a compound of the invention and a suitable powder base such as lactose or starch.
  • a proposed dose of the active compounds of the invention for oral, parenteral or buccal administration to the average adult human for the treatment of the conditions referred to above is 0.1 to 1000 mg of the active ingredient per unit dose which could be administered, for example, 1 to 4 times per day.
  • Aerosol formulations for treatment of the conditions referred to above are preferably arranged so that each metered dose or "puff' of aerosol contains 20 ⁇ g to 1000 ⁇ g of the compound of the invention.
  • the overall daily dose with an aerosol will be within the range 0.1 mg to 1000 mg.
  • Administration may be several times daily, for example 2, 3, 4 or 8 times, giving for example, 1 , 2 or 3 doses each time.
  • the active agents can be formulated for sustained delivery according to methods well known to those of ordinary skill in the art. Examples of such formulations can be found in United States Patents 3,538,214, 4,060,598, 4,173,626, 3,119,742, and 3,492,397 all of which are incorporated herein in their entireties for all purposes.
  • the compounds of the invention may also be utilized in combination therapy with other therapeutic agents such as Cyclosporin A, ISAtx247, Rapamycin, Everolimus, FK-506, Azathioprine, Mycophenolate mofetil, Mycophenolic acid, Daclizumab, Basiliximab, Muromonab, Horse anti-thymocyte globulin, Polyclonal rabbit antithymocyte globulin, Leflunomide, FK-778 (MNA-715), FTY-720, BMS- 188667 (CTLA4-lg), RG-1046 (CTLA4-lg), Prednisone, Prednisolone, Methylprednisolone suleptanate, Cortisone, Hydrocortisone, Methotrexate, Sulfasalazine, Etanercept, Infliximab, Adalimumab (D2E7), CDP-571 , CDP-870, Anakinra, NS
  • Particle Beam Mass Spectra were recorded on either a Hewlett Packard 5989®, utilizing chemical ionization (ammonium), or a Fisons (or MicroMass) Atmospheric Pressure Chemical Ionization (APCI) platform which uses a 50/50 mixture of acetonitrile/water.
  • Room or ambient temperature refers to 20-25 °C. All non-aqueous reactions were run under a nitrogen atmosphere for convenience and to maximize yields. Concentration in vacuo means that a rotary evaporator was used.
  • N-[(5-chloro-2- ⁇ 2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl- piperazin-1-yl]-2-oxo-ethoxy ⁇ -pyridin-3-yl)-acetic acid (0.045 g, 0.10 mmol) in dichloromethane (2 mL) was added 4-dimethylaminopyridine (0.018 g, 0.15 mmol), and 1 ,3-dicyclohexylcarbodiimide (0.023 g, 0.11 mmol).
  • Example 37 (2- ⁇ 2-r(2R)-2-Carbamoylmethyl-4-(4-fluoro-benzv0-piperazin-1-yl1-2-oxo- ethoxy)-5-chloro-phenoxy)-acetic acid r2-(4-fluoro-benzylamino)-ethyll-carbamic acid tert-butyl ester (2-Amino-ethyl)-carbamic acid tert-butyl ester (5.95 g, 37.1 mmol), 4- fluorobenzaldehyde (5.07 g, 40.9 mmol, 4.4 mL), triethylamine (1.50 g, 14.9 mmol, 2.1 mL) and magnesium sulfate (6.71 g, 55.7 mmol) were stirred in methanol (50 mL).
  • 6-(5-chloro-2- ⁇ 2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl- piperazin-1-yl]-2-oxo-ethoxy ⁇ -phenoxymethyl)-nicotinic acid methyl ester (0.13 g, 0.23 mmol) in 2:2:1 tetrahydrofuran:methanol:H 2 O (2 mL) was added lithium hydroxide hydrate (0.020 g, 0.48 mmol).
  • this compound was prepared by methods described in: Eur. J. Med. Chem. 1990, 25, 749) in ethanol was bubbled hydrogen chloride (g) for 10 minutes.

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Abstract

L'invention concerne des composés représentés par la formule (1) et des formes de ceux-ci pharmaceutiquement acceptables. Dans cette formule, X, Y, a, b, c. d, R?1, R2, R3, R4 et R5¿ sont tels que définis dans revendications. L'invention concerne également des compositions pharmaceutiques comprenant un composé représenté par la formule (I) et un excipient pharmaceutiquement acceptable. L'invention concerne enfin des méthodes d'utilisation des composés et compositions précités pour traiter ou prévenir un trouble ou un état par production d'effets antagonistes du récepteur 15 CCR1 chez un mammifère.
PCT/IB2002/003989 2001-10-22 2002-09-26 Derives de piperazine a activite antagoniste du recepteur ccr1 WO2003035627A1 (fr)

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JP2003538143A JP2005507923A (ja) 2001-10-22 2002-09-26 Ｃｃｒ１受容体アンタゴニスト活性を有するピペラジン誘導体
KR10-2004-7005885A KR20040047941A (ko) 2001-10-22 2002-09-26 Ｃｃｒ1 수용체 길항제 활성을 갖는 피페라진 유도체
APAP/P/2004/003008A AP2004003008A0 (en) 2001-10-22 2002-09-26 Piperazine derivatives with CCR1 receptor antagonist activity
EEP200400088A EE200400088A (et) 2001-10-22 2002-09-26 CCR1 retseptori suhtes antagonistlikku aktiivsustomavad piperasiiniderivaadid
SK185-2004A SK1852004A3 (sk) 2001-10-22 2002-09-26 Deriváty piperazínu s účinkami antagonistu receptora CCR1
DK02772651.2T DK1438298T3 (da) 2001-10-22 2002-09-26 Piperazin-derivater med CCR1 receptor-antagonist-aktivitet
EA200400466A EA006243B1 (ru) 2001-10-22 2002-09-26 Производные пиперазина с антагонистической активностью к рецептору ccr1
BR0213452-7A BR0213452A (pt) 2001-10-22 2002-09-26 Derivados de piperazina com atividade antagonista receptora de ccr1
HU0401735A HUP0401735A3 (en) 2001-10-22 2002-09-26 Piperazine derivatives with ccr1 receptor antagonist activity and pharmaceutical compositions containing them
CA002463272A CA2463272C (fr) 2001-10-22 2002-09-26 Derives de piperazine a activite antagoniste du recepteur ccr1
MXPA04002423A MXPA04002423A (es) 2001-10-22 2002-09-26 Derivados de piperazina con actividad antagonista del receptor ccr1.
EP02772651A EP1438298B1 (fr) 2001-10-22 2002-09-26 Derives de piperazine a activite antagoniste du recepteur ccr1
AT02772651T ATE456559T1 (de) 2001-10-22 2002-09-26 Piperazinderivate mit ccr1-rezeptor- antagonistischer wirkung
DE60235249T DE60235249D1 (de) 2001-10-22 2002-09-26 Piperazinderivate mit ccr1-rezeptor-antagonistischer wirkung
IS7180A IS7180A (is) 2001-10-22 2004-03-11 Píperasínafleiður með CCR1 viðtaka mótverkandi virkni
HR20040289A HRP20040289A2 (en) 2001-10-22 2004-03-23 Piperazine derivatives with ccr1 receptor antagonist activity
TNP2004000072A TNSN04072A1 (fr) 2001-10-22 2004-04-21 Derives de piperazine a activite des recepteur ccr1
NO20041631A NO20041631L (no) 2001-10-22 2004-04-21 Piperazinderivater med CCR1 reseptor antagonist

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FR2976943B1 (fr) * 2011-06-23 2013-07-12 Metabolys Derives de piperazine, leurs procedes de preparation et leurs utilisations dans le traitement de l'insulinoresistance
CN103012318B (zh) * 2012-11-25 2014-12-10 大理学院 氟苄基取代哌嗪类化合物及其制备和医药用途
CN113754616B (zh) * 2021-09-27 2023-07-18 北京工商大学 一种反式-3-苯硫基-γ-内酯的制备方法

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WO2021123813A1 (fr) 2019-12-18 2021-06-24 Cambridge Enterprise Limited Traitement et pronostic de cancer du pancréas

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HRP20040289A2 (en) 2004-10-31
US7098212B2 (en) 2006-08-29
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ZA200402090B (en) 2005-05-23
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EP1438298B1 (fr) 2010-01-27
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US20040034034A1 (en) 2004-02-19
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PA8556901A1 (es) 2003-11-12
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MXPA04002423A (es) 2004-05-31
DE60235249D1 (de) 2010-03-18
MA27142A1 (fr) 2005-01-03
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CA2463272A1 (fr) 2003-05-01
HUP0401735A3 (en) 2005-06-28
ATE456559T1 (de) 2010-02-15
EA200400466A1 (ru) 2004-08-26
JP2005507923A (ja) 2005-03-24
AR037742A1 (es) 2004-12-01
OA12670A (en) 2006-06-20
UY27503A1 (es) 2003-06-30
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CZ2004519A3 (cs) 2004-12-15
IL160974A0 (en) 2004-08-31
AP2004003008A0 (en) 2004-06-30
EE200400088A (et) 2004-10-15
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